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North American Rescue Products, Inc.
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JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088 is an FDA 510(k)-cleared medical device (K123194) manufactured by North American Rescue Products, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 2, 2013. Regulation: 8.